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Ethyl (Z)-2-cyano-3-(5-nitro-2-furyl)prop-2-enoate is a complex organic compound with the chemical formula C12H10N2O5. It is a derivative of ethyl 2-cyanoacrylate, featuring a 5-nitro-2-furyl group attached to the propenoate chain. This molecule is characterized by its (Z)-configuration, indicating the geometric arrangement of the double bond. It is known for its potential applications in various chemical and pharmaceutical processes, such as the synthesis of polymers and other specialty chemicals. The compound's structure and properties make it a subject of interest in organic chemistry research and development.

5410-94-6

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5410-94-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5410-94-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5410-94:
(6*5)+(5*4)+(4*1)+(3*0)+(2*9)+(1*4)=76
76 % 10 = 6
So 5410-94-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O5/c1-2-16-10(13)7(6-11)5-8-3-4-9(17-8)12(14)15/h3-5H,2H2,1H3/b7-5-

5410-94-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-cyano-3-(5-nitrofuran-2-yl)prop-2-enoate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:5410-94-6 SDS

5410-94-6Relevant academic research and scientific papers

Silica bonded N-(propylcarbamoyl)sulfamic acid (SBPCSA) as a highly efficient and recyclable solid catalyst for the synthesis of Benzylidene Acrylate derivatives: Docking and reverse docking integrated approach of network pharmacology

Aslam, Afroz,Parveen, Mehtab,Alam, Mahboob,Silva, Manuela Ramos,Silva, P.S. Pereira

, (2020/08/17)

A green approach has been developed for the synthesis of a series of benzylidene acrylate 3(a-p) from differently substituted aromatic/heterocyclic aldehydes and ethyl cyanoacetate in excellent yields (90–98%), and employing silica bonded N-(Propylcarbamoyl)sulfamic acid as a recyclable catalyst under solvent-free condition. The molecular structure of compounds 3b, 3d and 3i were well supported by single-crystal X-ray crystallographic analysis. The present protocol bears wide substrate tolerance and is believed to be more practical, efficient, eco-friendly, and compatible as compared to existing methods. In-silico approaches were implemented to find the biochemical and physiological effects, toxicity, and biological profiles of the synthesized compounds to determine the expected biological nature and confirm a drug-like compound. A molecular docking study of the expected biologically active compound was performed to know the hypothetically binding mode with the receptor. Also, reverse docking is applied to recognize receptors from unknown protein targets for drug-like compounds to explain poly-pharmacology and binding postures with different receptors.

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